Role
You will assist with the setup and co-ordination of trials, assist with provision of documentation to obtain appropriate ethical approval and assist with the writing of summary reports and publications, all under the supervision and direction of a trial co-ordinator and/or senior trial manager. This will involve liaising with members of the research team (including secretarial and administrative staff, trial managers, trial co-ordinators, data managers, statisticians, health economists and qualitative researchers).
This post is to work across several funded projects, the type of projects will partly depend upon the background and experience of the successful candidate.
Skills, Experience & Qualifications needed
1. Excellent communication skills and have the ability to assist with the set up and co-ordination of randomised controlled trials.
2. First degree in a relevant area and demonstrate a knowledge and understanding of healthcare, social science or education research.
3. Attention to detail and commitment to high quality
4. Knowledge of research methods, evaluative designs and randomised controlled trial methodologies to engage high quality research
5. Skilled in use of a range of computer software packages including Word, Excel, Power Point
Interview date: To be confirmed